enalapril maleate
Generic: enalapril maleate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
enalapril maleate
Generic Name
enalapril maleate
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
enalapril maleate 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4153
Product ID
70518-4153_3fb64f07-84a0-ce6c-e063-6394a90ac91b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075479
Listing Expiration
2026-12-31
Marketing Start
2024-08-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184153
Hyphenated Format
70518-4153
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
enalapril maleate (source: ndc)
Generic Name
enalapril maleate (source: ndc)
Application Number
ANDA075479 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-4153-0)
- 100 TABLET in 1 BOTTLE, PLASTIC (70518-4153-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3fb64f07-84a0-ce6c-e063-6394a90ac91b", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858810"], "spl_set_id": ["7077d32e-4b06-4d48-ba0c-6db2f8ebe08c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4153-0)", "package_ndc": "70518-4153-0", "marketing_start_date": "20240801"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-4153-1)", "package_ndc": "70518-4153-1", "marketing_start_date": "20250320"}], "brand_name": "Enalapril maleate", "product_id": "70518-4153_3fb64f07-84a0-ce6c-e063-6394a90ac91b", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "70518-4153", "generic_name": "Enalapril maleate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "20 mg/1"}], "application_number": "ANDA075479", "marketing_category": "ANDA", "marketing_start_date": "20240801", "listing_expiration_date": "20261231"}